2019
DOI: 10.1039/c9ra01554j
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Hyper-branched structure—an active carrier for copolymer with surface activity, anti-polyelectrolyte effect and hydrophobic association in enhanced oil recovery

Abstract: Herein, a hyper-branched polymer h-PMAD with, simultaneously, surface activity, an anti-polyelectrolyte effect and a hydrophobic association was prepared via aqueous solution free radical polymerization, and characterized by IR, NMR, TG–DTG and SEM.

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Cited by 9 publications
(9 citation statements)
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References 53 publications
(45 reference statements)
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“…7 The hydrophobic association is an endothermic process, which is boosted by heat intake and enhances the solution viscosity owing to the stretching of the macromolecular chain. 14 The viscosity−shear rate profiles show that the PPG hydrogel exhibits higher viscosity values compared to the PEG hydrogel. This behavior may be justified by increasing the hydrophobic carbon chain in the PPG skeleton, thus giving rise to solution viscosity rather than the PEG hydrogel.…”
Section: Resultsmentioning
confidence: 98%
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“…7 The hydrophobic association is an endothermic process, which is boosted by heat intake and enhances the solution viscosity owing to the stretching of the macromolecular chain. 14 The viscosity−shear rate profiles show that the PPG hydrogel exhibits higher viscosity values compared to the PEG hydrogel. This behavior may be justified by increasing the hydrophobic carbon chain in the PPG skeleton, thus giving rise to solution viscosity rather than the PEG hydrogel.…”
Section: Resultsmentioning
confidence: 98%
“…Moreover, the sulfonate groups boost the hydrogen bonding, thus enhancing the solution stability . The hydrophobic association is an endothermic process, which is boosted by heat intake and enhances the solution viscosity owing to the stretching of the macromolecular chain . The viscosity–shear rate profiles show that the PPG hydrogel exhibits higher viscosity values compared to the PEG hydrogel.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The most common modification in the chitosan structure was to include the branched segments and hydrophobic graft and they became amphiphilic by insertion of the copolymers. [26][27][28][29] A few works aimed to change the capillary force of the reservoir through use the of chitosan derivatives. Fe 3 O 4 @Chitosan nanocomposites were used as EOR additives in the carbonate's reservoir at HPHT conditions.…”
Section: Introductionmentioning
confidence: 99%
“…The second stage at 250-325C related to the disintegration of the amide groups on the hydrogel chains [5][6] . The third stage at 325-385C corresponds to the complete degradation of other side chain moieties, including sulfonic groups in AMPS and pyrrolidone rings, in addition to the breakdown of carbon-nitrogen bonds [6][7] . The fourth stage occurs at 385-600C and related to the complete degradation and carbonization of the polymer skeleton 6 .…”
Section: Figure S4: 1 H-nmr Of Peg-and Ppg-surfmers and Hydrogelsmentioning
confidence: 99%